Universal reference book for medicines
Name of the preparation: PHOSPHOGLIV ® (PHOSPHOGLIV)

Active substance: glycyrrhizinic acid, non welcome

Type: Hepatoprotector with immunomodulating and antiviral action

Manufacturer: FARMSTANDART-UfaVITA (Russia)
Composition, form of production and packaging
Liofilizate for the preparation of a solution for intravenous administration in the form of a mass from white to light yellow color.
1 f.
phospholipids (C 100 lipoid) 500 mg
sodium glycyrrhizinate (trisodium salt of glycyrrhizic acid) 200 mg
2.5 g - glass bottles (5) complete with water and water solvents (amp 10 ml 5 pcs.) - plastic contour packings (1) - cardboard packs.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2016.
PHARMACHOLOGIC EFFECT
Combined drug.
Has a membrane-stabilizing, hepatoprotective and antiviral effect.
Phosphatidylcholine (the main component of phospholipids) is the main structural element of cellular and intracellular membranes, capable of restoring their structure and functions in damage, providing a cytoprotective effect. Normalizes protein and lipid metabolism, prevents the loss of hepatocytes of enzymes and other active substances, restores the detoxifying function of the liver, inhibits the formation of connective tissue, reducing the risk of fibrosis and cirrhosis of the liver.
Glycyrrhizic acid has an anti-inflammatory effect, suppresses the reproduction of viruses in the liver and other organs by stimulating the production of interferons, increasing phagocytosis, increasing the activity of natural killer cells. Has a hepatoprotective effect due to antioxidant and membrane-stabilizing activity. Potentiates the action of endogenous glucocorticoids, providing anti-inflammatory and anti-allergic effects in non-infectious liver lesions.
When the skin is damaged due to the membrane-stabilizing and anti-inflammatory effect of the components, it limits the spread of the process and promotes regression of the disease.
INDICATIONS
- viral hepatitis (acute and chronic);
- fatty liver degeneration (hepatosis);
- other liver damage (medicinal, alcoholic, toxic);
- cirrhosis of the liver;
- intoxication;
- psoriasis;
- Neurodermatitis;
- Eczema.
DOSING MODE
Adults and children over 12 years: in / in, pre-dissolving the powder in 10 ml of water for injection. I / O administration should be slow. Enter 10 ml daily 2 times / day in the morning and in the evening for 10 days with the subsequent transition to oral administration of the drug in the form of capsules. The duration of the course can be increased on the recommendation of a doctor.
SIDE EFFECT
From the skin and subcutaneous tissues: with increased individual sensitivity, a skin rash may appear, which disappears after the drug is discontinued.
When the daily dose is exceeded: sodium and fluid retention, edema, increased blood pressure, hypokalemia are possible. If these symptoms appear, depending on their severity, it is necessary to reduce the dose of the drug and / or to prescribe spironolactone at 50-100 mg / day.
CONTRAINDICATIONS
- Pregnancy;
- the period of lactation (breastfeeding);
- children's age till 12 years;
- Hypersensitivity to the components of the drug.
PREGNANCY AND LACTATION
The drug is contraindicated for use in pregnancy and lactation (breastfeeding).
APPLICATION FOR VIOLATIONS OF THE FUNCTION OF KIDNEYS
Caution should be given to patients with portal hypertension.
APPLICATION FOR CHILDREN
Contraindication: children under 12 years.
DRUG INTERACTION
The contents of the vial should not be mixed with other solutions.
For dissolution use only water for injection.
Do not use saline solution of sodium chloride or glucose solution for dilution.
TERMS OF RELEASE FROM PHARMACY
The drug is released by prescription.
TERMS AND CONDITIONS OF STORAGE
The drug should be stored out of the reach of children, protected from light at a temperature of no higher than 20 ° C. Term - 2 years.
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